Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89632918-89633190 | Common:1; Rare:76 | ||||
chr1:89820889-89821204 | Common:1; Rare:99 | ||||
chr1:89994981-89995201 | Common:2; Rare:83 | ||||
chr1:91021461-91021683 | Common:2; Rare:51 | ||||
chr1:91021963-91022152 | Rare:54 | ||||
chr1:91500693-91500901 | Common:2; Rare:64 | ||||
chr1:91886099-91886333 | Rare:95 | ||||
chr1:92080303-92080567 | Common:3; Rare:66 | ||||
chr1:92298939-92299089 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr1:93079043-93079319 | Common:4; Rare:119 | ||||
chr1:93179879-93179954 | Common:1; Rare:18 | ||||
chr1:93180224-93180261 | Rare:14 | ||||
chr1:93180291-93180762 | Common:2; Rare:188 | ||||
chr1:93345754-93345912 | Common:4; Rare:63 | ||||
chr1:93448002-93448299 | Common:3; Rare:90 |